Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449825Generated: October 30, 2026

Dimethylformamide → HCID 66933293, compound

https://huagongshe.com/reaction/449825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHCID 66933350HCID 66933350—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystZinc AcetateHCID 11192—
CatalystZincHCID 23994—
CatalystPalladium ChlorideHCID 24290—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
ProductHCID 66933293HCID 6693329369%

Reaction Steps

The following reagents are stirred together in DMF (250 mL) at 100° C. for 18 h: ((S)-7-bromo-1,2,3,4-tetrahydro-cyclopenta[b]indol-2-yl)-carbamic acid tert-butyl ester (50.0 g, 142 mmol), zinc cyanide (11.9 g, 99.7 mmol), zinc acetate (5.22 g, 28.5 mmol), 1,1′-bis(diphenylphosphino)ferrocene)palladium (II) chloride (Pd(dppf)2Cl2) (1.74 g, 2.14 mmol), and zinc (3.72 g, 56.9 mmol). The reaction is concentrated to dryness and partitioned between water and ethyl acetate. The organics are washed with water and brine, then concentrated to afford a solid. The solid is chromatographed in two equal portions on silica gel (1600 mL) as follows: load as a solution in CH2Cl2 and elute with 2% EtOAc in CH2Cl2 (3 L), then 5% EtOAc in CH2Cl2. The product is recovered from the two columns to give 29 g (69%) of the title compound as a white solid. 1H-NMR (400 MHz, CDCl3) δ 8.39 (s, 1H), 7.74 (s, 1H), 7.34 (d, J=1.8 Hz, 2H), 5.05-4.96 (m, 2H), 3.37-3.25 (m, 2H), 2.80-2.63 (m, 2H), 1.46 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486943B2
Source datasetuspto-grants-2013_07
ORD IDord-7d4ee2a6a9d3414a8e28b85dd9afdf6f
Source noteuspto-grants-2013_07